management of hyperemesis gravidarum guidelines - copy

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DR. MEENAKSHI SHARMA DR. SHARDA JAIN DR. JYOTI BHASKAR DR. JYOTI AGARWAL MANAGEMENT OF HYPEREMESIS GRAVIDARUM LATEST GUIDELINES UPDATE

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DR. MEENAKSHI SHARMA DR. SHARDA JAIN DR. JYOTI BHASKAR DR. JYOTI AGARWAL

MANAGEMENT OF

HYPEREMESIS GRAVIDARUM LATEST GUIDELINES UPDATE

2015

Our Gift to Doctor’s Community

Review this Lecture and others at:Slideshare.net/lifecarecentre

MANAGEMENT OF

HYPEREMESIS GRAVIDARUM LATEST GUIDELINES UPDATE

MANAGEMENT OF

HYPEREMESIS GRAVIDARUM -

GUIDELINES

Dr Meenakshi Sharma

Dr. Sharda Jain

Dr. Jyoti Bhaskar

Dr. Jyoti Agarwal NICE 2013

ACOG 2010

SOGC 2002

HYPEREMESIS GRAVIDARUM

Severe nausea & intractable vomiting

Affects - 0.3-2% of pregnancies

PATHOPHYSIOLOGY Pathophysiology – multifactorial

HCG– increased levels in pts with HG as HCG stimulates secretions in upper GIT

Estrogen- positive assoc b/w NVP and maternal serum E2 level. Increased E2 causes a decrease in GI motility and gastric emptying altering GI pH and encourages subclinical H pylori infection

Thyroid hormone- physiological gestational transient thyrotoxicosis. Raised FT3 & low TSH found in 66% HG

Symptoms

NauseaVomitingEnhanced olfactory sensesFood and/or fluid intoleranceLethargy

HYPEREMESIS GRAVIDARUM

HYPEREMESIS GRAVIDARUM

Signs

DehydrationWeight lossKetonuriaAnaemiaTachycardia

HYPEREMESIS GRAVIDARUM

HYPEREMESIS GRAVIDARUM

Initial InvestigationsUrea and ElectrolytesLFTCBCUrinalysisUSG-multiple/molar pregnancies

Additional investigationsCalciumBlood sugarTSH

HYPEREMESIS GRAVIDARUM

HYPEREMESIS GRAVIDARUM

COMPLICATIONS Maternal

Hypokalemia Hyponatremia and central pontine myelinosis Wernickie’s encephalopathy Vitamin B6/B12 deficiency Malnutrition Mallory- Weiss esophageal tears Venous thromboembolism Psychological morbidity

Fetal Growth restriction Wernicke’s encephalopathy is associated with

40% fetal death

COMPLICATIONS

Hyponatremia (Na<120 mmol/l) - anorexia, headache, nausea, vomiting and lethargy

Severe hyponatremia may lead to central pontine myelinolysis (osmotic demyeliniation) Pyramidal tract signs Spastic quadriparesis Pseudobulbar palsy Altered sensorium Ataxia and convulsion

It is medical emergency Should be managed

appropriately by skilled personnel

As treatment may be potentially as dangerous as the condition itself

Vitamin B1 deficiency precipitated by IV fluid containing high concentration of dextrose Ophthalmoplegia (typically sixth nerve palsy,

diploia), Ataxia Altered sensorium

Diagnosis confirmed by low red cell transketolase, a thiamine dependent enzyme

MRI - symmetrical lesion around the aqueduct and fourth ventricle, which resolve after treatment with thiamine

TREATMENT

Thiamine replacement may improve the symptoms of Wernicke’s encephalopathy

if associated with Korsakoff psychosis (retrograde amnesia, impaired ability to learn and confabulation) the recovery rate is only about 50%

40% incidence of fetal death

Differential Diagnosis System

Diagnosis

Genitourinary UTI Uraemia Molar pregnancy

Gastrointestinal Gastritis/ peptic ulcer Reflux/ oesophagitis Pancreatitis Bowel obstruction

Endocrine Addison’s disease Hyperthyroidism Diabetes ketoacidosis

CNS Intracranial tumours Vestibular disease

Correction of dehydration and electrolyte imbalance

Prophylaxis against recognized complications

Provision of symptomatic relief

Admit if :Symptom are severe despite 24 hrs of

medicationEvidence of dehydration and ketosisAdmit earlier if coexisting conditions eg

diabetes

IV fluid- NS and Hartmann’s solution preferrable if ketotic or fluid intolerant

Avoid dextrose solution as can’t correct commonly associated

hyponatraemia High conc of dextrose solution

precipitate Wernicke’s encephalopathy

Avoid double strength saline even in cases of severe hyponatraemia

Antiemetics are safe and recommended liberally in HG

Pts on antiemetic -better pregnancy outcome due to better nutrition

REMEMBER !!!!! MEDICATION TO BE KEPT TO MINIMUM

Class of drugs Antiemetic

Phenothiazine Prochlorperazine (stemetil/ buccastem) Chlorpromazine

Dopamine antagonists Metoclopramide Domperidone

5-HT3 (serotonin) antagonist Ondansetron

Antihistamines (H1 receptor antagonist)

Cyclizine Promethazine (phenergan) Meclozine

Group One Dose Route

First line Cyclizine 50 mg t.d.s. PO, IM or IV

Second line Prochlorperazine (Stemetil)

12.5 mg t.d.s. 3-6 mg b.d

IM sublingual

Third line Metoclopramide 10 mg t.d.s. PO, IM or IV

Group two:

Promethazine (phenergan)

25 mg a day IM/oral

Chlorpromazine 10-25 mg t.d.s. 25 mg t.d.s.

PO

Domperidone 20 mg qds 30-60 mg qds

PO PR

Steroids should be used for intractable hyperemesis which is not responding to above management

I/V Hydrocortisone 100 mg BD for 48 hrs

Oral prednisolone 30 – 40 mg/day -1 week then tapered gradually 5mg reduction every week

Increased risk of VTE due to dehydration and immobilization in hospitalized pts.

LMWH should be given if the risk factor score for VTE is 3 or more

Pre-existing risk factors Score

Previous recurrent VTE 3

Previous unprovoked or estrogen related

3

Previous VTE provoked 2

Family history of VTE 1

Known thrombophilia 2

Medical comorbidity 2

Age (> 35 years) 1

Obesity 1 or 2 *

Parity (≥ 3) 1

Smoker 1

Gross varicose vein 1

Obstetric risk factors 1

Pre-eclampsia 1

Dehydration/ Hyperemesis/ OHSS

1

Multiple pregnancy or ART 1

Transient risk factors

Current systemic infection 1

Immobility 1

Surgical procedure in pregnancy

2

Total score

Risk assessment for Venous

Thromboembolism (VTE)

*Score 1 for BMI >30 *Score 2 for BMI >40

Prolonged nausea & vomiting Intolerable to fluid and/or food Clinical dehydration Ketouria Weight loss

Nausea & vomiting History of other medical condition e.g diabetes,

Summary for Management of Hyperemesis Gravidarum-NHS 2013

Admission

Admission

Initial assessment Temp, Pulse, Resp, BP, Body weight U&E LFT Urinalysis/ MSU USS

Additional investigations FBC (full blood count) Blood glucose TFT (thyroid function test) Calcium

Diagnosis

Treatment

Subsequent assessment Fluid intake output chart

U&E (urea and electrolytes), LFT (liver function test

Alternate day if initial results were normal, daily if the results

were abnormal

Fluid & electrolyte replacement Normal saline/

Hartmann’s 3 litres/day

KCl (potassium/ about 100 mmol/24

hr)

All hyperemesis Pabrinex 250 mg thiamine per pair

weekly if oral thiamine is not

tolerated. Clexane (as per

protocol)

Antiemetics (1st group) 1st line: Cyclizine 50 mg t.d.s. PO, IM or IV2nd line: Prochlorperazine 12.5mg t.d.s. IM Buccastem 3-6mg bd sublingually

Third line: Metoclopramide 10 mg t.d.s. PO IM or IV

Intractable vomiting

Antiemetics (2nd group)

Promethazine (phenergan) 25 mg a

day IM/oral Chlorpromazine 10-25

mg t.d.s. PO 25 mg t.d.s. IM

Domperidone 10 mg q.d.s PO

30-60 mg b.d PR

With consultant decision

Ondansetron 4-8 mg b.d. PO, IM or IV

Hydrocortisone 100 mg b.d. IV for 48 hr followed

by: Prednisolone 30-40 mg

o.d. PO for one week then reduce the dose by 5

mg/week

Other supportive treatment

• Diet & lifestyle (small frequent dry meal, learn to avoid certain scents which make the patient intolerable)

• Ginger • Acupressure/

acupuncture  

The options for severe hyperemesis who failed to response to above measures

• Enteral nutrition• Parenteral nutrition

(TPN)• Termination of

pregnancy

A doxylamine/pyridoxine combination should be the standard of care, since it has the greatest evidence to support its efficacy and safety. (I-A)

H1 receptor antagonists should be considered in the management of acute or breakthrough episodes of NVP. (I-A)

Pyridoxine monotherapy supplementation may be considered as an adjuvant measure. (I-A)

Phenothiazines are safe and effective for severe NVP. (I-A)

SOGC 2002, ACOG 2010

HYPEREMESIS GUIDELINES Metoclopramide is safe to be used for

management of NVP, although evidence for efficacy is more limited. (II-2D)

Corticosteroids should be avoided during the first trimester because of possible increased risk of oral clefting and should be restricted to refractory cases. (I-B)

When NVP is refractory to initial pharmacotherapy, investigation of other potential causes should be undertaken. (III-A)

SOGC 2002, ACOG 2010

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